美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA091672"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
85509-1396-3 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-3)
85509-1396-6 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-6)
85509-1396-9 85509-1396 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250723 N/A ANDA ANDA091672 PHOENIX RX LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1396-9)
71610-280-30 71610-280 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250827 N/A ANDA ANDA091672 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-280-30)
71610-280-53 71610-280 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250827 N/A ANDA ANDA091672 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-280-53)
71610-280-60 71610-280 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190522 N/A ANDA ANDA091672 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-280-60)
71610-280-80 71610-280 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250827 N/A ANDA ANDA091672 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 40 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-280-80)
68071-4024-3 68071-4024 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170728 N/A ANDA ANDA091672 NuCare Pharmaceuticals,Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-4024-3)
0615-8079-05 0615-8079 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20141031 N/A ANDA ANDA091672 NCS HealthCare of KY, LLC dba Vangard Labs OMEPRAZOLE 40 mg/1 15 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8079-05)
76420-878-00 76420-878 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241203 N/A ANDA ANDA091672 Asclemed USA, Inc. OMEPRAZOLE 10 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-00)
76420-878-01 76420-878 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241203 N/A ANDA ANDA091672 Asclemed USA, Inc. OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-01)
76420-878-03 76420-878 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241203 N/A ANDA ANDA091672 Asclemed USA, Inc. OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-03)
76420-878-06 76420-878 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241203 N/A ANDA ANDA091672 Asclemed USA, Inc. OMEPRAZOLE 10 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-06)
76420-878-09 76420-878 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241203 N/A ANDA ANDA091672 Asclemed USA, Inc. OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-878-09)
70518-0199-0 70518-0199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170206 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0199-0)
70518-0199-1 70518-0199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170302 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-0199-1)
70518-0199-2 70518-0199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20220606 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0199-2)
70518-0199-4 70518-0199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250708 N/A ANDA ANDA091672 REMEDYREPACK INC. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-0199-4)
68071-2199-4 68071-2199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170329 N/A ANDA ANDA091672 NuCarePharmaceuticals, Inc. OMEPRAZOLE 40 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-4)
68071-2199-6 68071-2199 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170329 N/A ANDA ANDA091672 NuCarePharmaceuticals, Inc. OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-6)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase